論文

査読有り 国際誌
2016年10月

Hypoxia-induced increases in serotonin-immunoreactive nerve fibers in the medulla oblongata of the rat.

Acta histochemica
  • Ryosuke Morinaga
  • ,
  • Nobuaki Nakamuta
  • ,
  • Yoshio Yamamoto

118
8
開始ページ
806
終了ページ
817
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.acthis.2016.10.004

Hypoxia induces respiratory responses in mammals and serotonergic neurons in the medulla oblongata participate in respiratory control. However, the morphological changes in serotonergic neurons induced by hypoxia have not yet been examined and respiratory controls of serotonergic neurons have not been clarified. We herein investigated the distribution of immunoreactivity for serotonin (5-hydroxytryptamine; 5-HT) in the medulla oblongata of control rats and rats exposed to 1-6h of hypoxia (10% O2). We also examined the medulla oblongata by multiple immunofluorescence labeling for 5-HT, neurokinin 1 receptors (NK1R), a marker for some respiratory neurons in the pre-Bötzinger complex (PBC), and dopamine β-hydroxylase (DBH), a marker for catecholaminergic neurons. The number of 5-HT-immunoreactive nerve cell bodies in the raphe nuclei was higher in rats exposed to hypoxia than in control rats. The number of 5-HT-immunoreactive nerve fibers significantly increased in the rostral ventrolateral medulla of rats exposed to 1-6h of hypoxia, caudal ventrolateral medulla of rats exposed to 2-6h of hypoxia, and lateral part of the nucleus of the solitary tract and dorsal motor nucleus of the vagus nerve of rats exposed to 1-2h of hypoxia. Multiple immunofluorescence labeling showed that 5-HT-immunoreactive nerve fibers were close to NK1R-immunoreactive neurons in ventrolateral medulla and to DBH-immunoreactive neurons in the medulla. These results suggest that serotonergic neurons partly regulate respiratory control under hypoxic conditions by modulating the activity of NK1R-expressing and catecholaminergic neurons.

リンク情報
DOI
https://doi.org/10.1016/j.acthis.2016.10.004
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/27825705
ID情報
  • DOI : 10.1016/j.acthis.2016.10.004
  • PubMed ID : 27825705

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